chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	207602884	207602887	ACA	---	3	GENIC	homozygous	59265643
4	207603195	207603196	C	T	11	GENIC	possibly homozygous	57065166
4	207603953	207603954	A	G	18	GENIC	homozygous	57065169
4	207604642	207604643	G	A	17	GENIC	homozygous	59265645
4	207607653	207607654	G	A	7	GENIC	homozygous	59265647
4	207608536	207608537	C	A	19	GENIC	possibly homozygous	59265649
4	207608618	207608619	A	C	14	GENIC	homozygous	59265651
4	207608969	207608970	T	G	18	GENIC	possibly homozygous	57065178
4	207609015	207609016	T	G	17	GENIC	possibly homozygous	59265653
4	207609367	207609368	A	AC	15	GENIC	possibly homozygous	59265655
4	207609423	207609424	T	C	7	GENIC	homozygous	57065180
4	207609847	207609848	T	G	10	GENIC	heterozygous	59265657
4	207609848	207609849	T	C	10	GENIC	heterozygous	59265659
4	207610168	207610169	A	G	4	GENIC	heterozygous	57065181
4	207612375	207612376	A	-	7	GENIC	homozygous	57065184
4	207612796	207612797	A	G	8	GENIC	homozygous	57065185
4	207612816	207612817	C	T	12	GENIC	homozygous	59265663
4	207612904	207612905	A	AG	7	GENIC	homozygous	57065186
4	207616210	207616211	G	T	19	GENIC	possibly homozygous	57065188
4	207617257	207617258	A	G	15	GENIC	possibly homozygous	59265665
4	207618061	207618062	C	T	8	GENIC	homozygous	58094216
4	207618209	207618210	G	A	20	GENIC	homozygous	58094218
4	207618516	207618517	A	T	10	GENIC	possibly homozygous	59265667
4	207619573	207619574	G	A	16	GENIC	homozygous	59265669
4	207620910	207620911	A	G	13	GENIC	homozygous	57065191
4	207621611	207621612	A	G	19	GENIC	homozygous	57065192
4	207622844	207622845	A	ATGTC	4	GENIC	homozygous	57065194